Food & Drink / Compounds / Daidzein

Daidzein in food: ingestion safety

Low risk

(People-specific data is limited; this page draws from human adult context.) Second major soy isoflavone; weaker ER binding than genistein. Metabolized to equol by gut bacteria (~30-50% of Western adults). Equol producers may have enhanced estrogenic/anti-estrogenic effects.

What is daidzein?

The IUPAC name is 7-hydroxy-3-(4-hydroxyphenyl)chromen-4-one.

Also known as: 4',7-Dihydroxyisoflavone, Daidzeol, 7-hydroxy-3-(4-hydroxyphenyl)-4H-chromen-4-one, 7,4'-Dihydroxyisoflavone.

IUPAC name
7-hydroxy-3-(4-hydroxyphenyl)chromen-4-one
CAS number
486-66-8
Molecular formula
C15H10O4
Molecular weight
254.24 g/mol
SMILES
Oc1ccc(-c2coc3cc(O)ccc3c2=O)cc1
PubChem CID
5281708

Risk for people

Low risk

Second major soy isoflavone; weaker ER binding than genistein. Metabolized to equol by gut bacteria (~30-50% of Western adults). Equol producers may have enhanced estrogenic/anti-estrogenic effects.

Regulatory consensus

2 regulatory and scientific bodies have classified Daidzein. The classifications differ — that's the data.

AgencyYearClassificationNotes
FDA1999GRAS as component of soy foods
EFSA2015No safety concern at dietary levels

Regulators apply different standards of evidence — animal-data weighting, exposure-pattern assumptions, epidemiological power thresholds — which is why two scientific bodies can review the same data and reach different conclusions. The disagreement is the data.

Where you encounter daidzein

  • Food
  • Dietary Supplement

Safer alternatives

Lower-risk approaches that achieve a similar outcome to Daidzein:

  • S-equol supplement (direct metabolite)
    Trade-offs: Only 30-50% of Western populations produce equol naturally from daidzein. Direct supplementation bypasses this. Limited clinical data.
    Relative cost: 3-5×

Frequently asked questions

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Look up products containing daidzein, compare to alternatives, and explore the full data record.

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Sources (1)

Reference data, not professional advice. Aggregates publicly available regulatory and scientific data; not a substitute for veterinary, medical, legal, or regulatory advice. Why we built ALETHEIA →